The Management of Nausea and Vomiting

of Pregnancy and Hyperemesis Gravidarum

Green-top Guideline No. 69

June 2016
The Management of Nausea and Vomiting of
Pregnancy and Hyperemesis Gravidarum
This is the first edition of this guideline.

Executive summary of recommendations

Diagnosis of nausea and vomiting of pregnancy (NVP) and hyperemesis gravidarum (HG)
How is NVP diagnosed?

NVP should only be diagnosed when onset is in the first trimester of pregnancy and other causes of
nausea and vomiting have been excluded.
D

How is HG diagnosed?

HG can be diagnosed when there is protracted NVP with the triad of more than 5% prepregnancy
weight loss, dehydration and electrolyte imbalance.
D

How can the severity of NVP be classified?

An objective and validated index of nausea and vomiting such as the Pregnancy-Unique
Quantification of Emesis (PUQE) score can be used to classify the severity of NVP.
C

What initial clinical assessment and baseline investigations should be done before deciding
on treatment?

P
Clinicians should be aware of the features in history, examination and investigation that allow NVP
and HG to be assessed and diagnosed and for their severity to be monitored.

What are the differential diagnoses?

P
Other pathological causes should be excluded by clinical history, focused examination and
investigations.

What is the initial management of NVP and HG?

How should the woman be managed?

Women with mild NVP should be managed in the community with antiemetics.
D
Ambulatory daycare management should be used for suitable patients when community/primary
C
care measures have failed and where the PUQE score is less than 13.

P
Inpatient management should be considered if there is at least one of the following:

continued nausea and vomiting and inability to keep down oral antiemetics
continued nausea and vomiting associated with ketonuria and/or weight loss (greater than 5%
of body weight), despite oral antiemetics
confirmed or suspected comorbidity (such as urinary tract infection and inability to tolerate
oral antibiotics).

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What therapeutic options are available for NVP and HG?

What is the safety and efficacy of pharmacological agents?

Antiemetics

There are safety and efficacy data for first-line antiemetics such as antihistamines (H1 receptor
antagonists) and phenothiazines and they should be prescribed when required for NVP and HG
C
(Appendix III).

P
Combinations of different drugs should be used in women who do not respond to a single antiemetic.

P
For women with persistent or severe HG, the parenteral or rectal route may be necessary and more
effective than an oral regimen.

Women should be asked about previous adverse reactions to antiemetic therapies. Drug-induced
extrapyramidal symptoms and oculogyric crises can occur with the use of phenothiazines and
B
metoclopramide. If this occurs, there should be prompt cessation of the medications.

Clinicians should use antiemetics with which they are familiar and should use drugs from different
classes if the first drug is not effective.
B

Metoclopramide is safe and effective, but because of the risk of extrapyramidal effects it should be
B
used as second-line therapy.

There is evidence that ondansetron is safe and effective, but because data are limited it should be
used as second-line therapy.
C

Pyridoxine

Pyridoxine is not recommended for NVP and HG.

C
Corticosteroids

Corticosteroids should be reserved for cases where standard therapies have failed.
A
Diazepam

Diazepam is not recommended for the management of NVP or HG.

B
What is the best rehydration regimen for ambulatory daycare and inpatient management?

Normal saline with additional potassium chloride in each bag, with administration guided by daily
monitoring of electrolytes, is the most appropriate intravenous hydration.
D

Dextrose infusions are not appropriate unless the serum sodium levels are normal and thiamine
has been administered.
D

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Which complementary therapies could be helpful?

Ginger

Ginger may be used by women wishing to avoid antiemetic therapies in mild to moderate NVP. A
Acustimulations acupressure and acupuncture

Women may be reassured that acustimulations are safe in pregnancy. Acupressure may improve
NVP.
B

Hypnosis

Hypnotic therapies should not be recommended to manage NVP and HG.

D
Monitoring and adverse effects
What complications or adverse effects can occur from NVP and HG and what are their preventive/
management strategies?

P
Urea and serum electrolyte levels should be checked daily in women requiring intravenous fluids.

Histamine H2 receptor antagonists or proton pump inhibitors may be used for women developing
D
gastro-oesophageal reflux disease, oesophagitis or gastritis.

Thiamine supplementation (either oral or intravenous) should be given to all women admitted with
D
prolonged vomiting, especially before administration of dextrose or parenteral nutrition.

Women admitted with HG should be offered thromboprophylaxis with low-molecular-weight heparin

C
unless there are specific contraindications such as active bleeding. Thromboprophylaxis can be
discontinued upon discharge.

Women with previous or current NVP or HG should consider avoiding iron-containing preparations
if these exacerbate the symptoms.
D

Further management
What is the role of the multidisciplinary team?

In women with severe NVP or HG, input may be required from other professionals, such as midwives,
nurses, dieticians, pharmacists, endocrinologists, nutritionists and gastroenterologists, and a
D
mental health team, including a psychiatrist.

When should enteral and parenteral nutrition be considered and what are the risks to the mother and
fetus?

When all other medical therapies have failed, enteral or parenteral treatment should be considered
D
with a multidisciplinary approach.

When should termination of pregnancy be considered?

All therapeutic measures should have been tried before offering termination of a wanted pregnancy.
D

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Discharge and follow-up
What discharge and follow-up arrangements should be implemented?

P
Women with NVP and HG should have an individualised management plan in place when they are
discharged from hospital.

Women with severe NVP or HG who have continued symptoms into the late second or the third
trimester should be offered serial scans to monitor fetal growth.
C

What is the effect of NVP and HG in the postnatal period?

How should we advise about future pregnancies?

Women with previous HG should be advised that there is a risk of recurrence in future pregnancies.
D
Early use of lifestyle/dietary modifications and antiemetics that were found to be useful in the index
pregnancy is advisable to reduce the risk of NVP and HG in the current pregnancy.
C

What is the effect of NVP and HG on quality of life?

A womans quality of life can be adversely affected by NVP and HG and practitioners should address
the severity of a womans symptoms in relation to her quality of life and social situation.
C

Practitioners should assess a womans mental health status during the pregnancy and postnatally
and refer for psychological support if necessary.
D

Women should be referred to sources of psychosocial support.

D
Practitioners should validate the womans physical symptoms and psychological distress.
C
Women should be advised to rest as required to alleviate symptoms.
D
1. Purpose and scope

There is variation in the management of women who have nausea and vomiting of pregnancy (NVP) or
hyperemesis gravidarum (HG) with an occasional lack of understanding of its severity and options for
treatment and support.

The aim of this guideline is to provide evidence-based or best clinical practice information regarding the
diagnosis and subsequent management of NVP and HG across community, ambulatory daycare and
inpatient settings. It gives advice for multidisciplinary professionals involved in the care of women with
these conditions, including how to counsel and support women before, during and after their pregnancies.

2. Introduction and background epidemiology

NVP affects up to 80% of pregnant women1 and is one of the most common indications for hospital
admission among pregnant women, with typical stays of between 3 and 4 days.24 For this guideline, NVP
is defined as the symptom of nausea and/or vomiting during early pregnancy where there are no other
causes. HG is the severe form of NVP, which affects about 0.33.6% of pregnant women.1,57 Reported HG
recurrence rates vary, from 15.2% in a Norwegian hospital registry study8 to 81% if using self-reported
diagnosis.9

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The aetiological theories for NVP and HG range from the fetoprotective and genetic to the biochemical,
immunological and biosocial.10,11 They are primarily thought to be associated with rising levels of beta
human chorionic gonadotrophin (hCG) hormone, and conditions with higher hCG levels, such as
trophoblastic disease and multiple pregnancy, have been associated with increased severity of NVP.12,13

3. Identification and assessment of evidence

This guideline was developed in accordance with standard methodology for producing Royal College of
Obstetricians and Gynaecologists (RCOG) Green-top Guidelines. Databases searched included the
Cochrane Library, EMBASE and MEDLINE. The databases were searched using the relevant Medical Subject
Headings (MeSH) terms, including all subheadings, and this was combined with a keyword search. Search
terms included nausea and vomiting, vomiting, nausea, hyperemesis, morning sickness, antiemetic
agent, fluids and hydration. The search was inclusive of all relevant articles published up to August 2015.
The National Guideline Clearinghouse, National Institute for Health and Care Excellence (NICE) Evidence
Search, Trip, Guidelines International Network and Geneva Foundation for Medical Education and Research
website were also searched for relevant guidelines and reviews.

Where possible, recommendations are based on available evidence. Areas lacking evidence are highlighted
and annotated as good practice points. Further information about the assessment of evidence and the
grading of recommendations may be found in Appendix I.

4. Diagnosis of NVP and HG

4.1 How is NVP diagnosed?

NVP should only be diagnosed when onset is in the first trimester of pregnancy and other causes of
nausea and vomiting have been excluded.
D

Onset of NVP is in the first trimester and if the initial onset is after 10+6 weeks of gestation, other
causes need to be considered. It typically starts between the fourth and seventh weeks of Evidence
gestation, peaks in approximately the ninth week and resolves by the 20th week in 90% of level 2

women.14

4.2 How is HG diagnosed?

HG can be diagnosed when there is protracted NVP with the triad of more than 5% prepregnancy
weight loss, dehydration and electrolyte imbalance.
D

HG is characterised by severe, protracted nausea and vomiting associated with weight loss of Evidence
more than 5% of prepregnancy weight, dehydration and electrolyte imbalances.7 level 2

4.3 How can the severity of NVP be classified?

An objective and validated index of nausea and vomiting such as the Pregnancy-Unique
Quantification of Emesis (PUQE) score can be used to classify the severity of NVP.
C

Objective, validated measures for the severity of nausea and vomiting include the Rhodes Index
and the PUQE index. The Rhodes Index15,16 was originally validated to measure nausea and
vomiting in chemotherapy patients, including assessment of physical symptoms and the resulting Evidence
stress, but has subsequently been used for NVP. A shorter disease-specific questionnaire (PUQE) level 2+

was developed by the Motherisk Program,17 an NVP helpline in Canada, which highly correlated
with the Rhodes Index.18 The PUQE was modified to include symptom profile over the previous

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24 hours including a wellbeing score that correlated with hydration status and, more recently,
Evidence
over a longer period of time.19,20 The PUQE score can be used to determine whether the NVP is level 2+
mild, moderate or severe (Appendix II) and can be used to track progress with treatment.

5. What initial clinical assessment and baseline investigations should be done before deciding
on treatment?

P
Clinicians should be aware of the features in history, examination and investigation that allow NVP
and HG to be assessed and diagnosed and for their severity to be monitored.

Table 1. Features in the history, examination and investigations to monitor severity and other causes

History Previous history of NVP/HG

Quantify severity using PUQE score: nausea, vomiting, hypersalivation, spitting, loss of weight,
inability to tolerate food and fluids, effect on quality of life
History to exclude other causes:
abdominal pain
urinary symptoms
infection
drug history
chronic Helicobacter pylori infection

Examination Temperature
Pulse
Blood pressure
Oxygen saturations
Respiratory rate
Abdominal examination
Weight
Signs of dehydration
Signs of muscle wasting
Other examination as guided by history

Investigation Urine dipstick:

quantify ketonuria as 1+ ketones or more
MSU
Urea and electrolytes:
hypokalaemia/hyperkalaemia
hyponatraemia
dehydration
renal disease
Full blood count:
infection
anaemia
haematocrit
Blood glucose monitoring:
exclude diabetic ketoacidosis if diabetic
Ultrasound scan:
confirm viable intrauterine pregnancy
exclude multiple pregnancy and trophoblastic disease
In refractory cases or history of previous admissions, check:
TFTs: hypothyroid/hyperthyroid
LFTs: exclude other liver disease such as hepatitis or gallstones, monitor malnutrition
calcium and phosphate
amylase: exclude pancreatitis
ABG: exclude metabolic disturbances to monitor severity

ABG arterial blood gas; LFTs liver function tests; MSU midstream urine; TFTs thyroid function tests.

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Reported HG recurrence rates vary, from 15.2% in a Norwegian hospital registry study8 to 81%
if using self-reported diagnosis.9 However, the incidence of HG reduces in a second pregnancy Evidence
if there is a change in paternity (10.9%) compared with no change (16%; adjusted OR 0.6, level 2+

95% CI 0.390.92).8,21

NVP and HG are associated with hyponatraemia, hypokalaemia, low serum urea, raised
haematocrit and ketonuria with a metabolic hypochloraemic alkalosis. If severe, a metabolic
acidaemia may develop. In two-thirds of patients with HG, there may be abnormal thyroid
function tests (based on a structural similarity between thyroid-stimulating hormone [TSH] and Evidence
hCG) with a biochemical thyrotoxicosis and raised free thyroxine levels with or without a level 2

suppressed thyroid stimulating hormone level. These patients rarely have thyroid antibodies
and are euthyroid clinically. The biochemical thyrotoxicosis resolves as the HG improves22 and
treatment with antithyroid drugs is inappropriate.

Liver function tests are abnormal in up to 40% of women with HG,23 with the most likely
abnormality being a rise in transaminases. Bilirubin levels can be slightly raised but without Evidence
jaundice, and amylase levels can be mildly raised too. These abnormalities improve as the HG level 3

resolves.

An ultrasound scan should be scheduled to confirm viability and gestational age and to rule out multiple
pregnancy or trophoblastic disease. Unless there are other medical reasons for an urgent scan, this can be
scheduled for the next available appointment as long as the NVP has resolved with treatment.

5.1 What are the differential diagnoses?

P
Other pathological causes should be excluded by clinical history, focused examination and
investigations.

Other pathological causes of nausea and vomiting include peptic ulcers, cholecystitis,
gastroenteritis, hepatitis, pancreatitis, genitourinary conditions such as urinary tract infection Evidence
or pyelonephritis, metabolic conditions, neurological conditions and drug-induced nausea and level 3

vomiting.2426

Severe abdominal or epigastric pain is unusual in NVP and HG and may warrant further investigation of
serum amylase levels and an abdominal ultrasound, and possibly oesophageal gastroduodenoscopy,
which is considered safe in pregnancy.

Chronic infection with Helicobacter pylori can be associated with NVP and HG and testing for Evidence
H. pylori antibodies may be considered.27,28 level 2+

6. What is the initial management of NVP and HG?

6.1 How should the woman be managed?

Women with mild NVP should be managed in the community with antiemetics.
D
Ambulatory daycare management should be used for suitable patients when community/primary
C
care measures have failed and where the PUQE score is less than 13.

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 P
Inpatient management should be considered if there is at least one of the following:

continued nausea and vomiting and inability to keep down oral antiemetics
continued nausea and vomiting associated with ketonuria and/or weight loss (greater than 5%
of body weight), despite oral antiemetics
confirmed or suspected comorbidity (such as urinary tract infection and inability to tolerate
oral antibiotics).

Since most women with NVP require only oral antiemetics, management in the community/
primary care is appropriate to avoid unnecessary hospital admissions and disruption to the Evidence
womans life.29 Women who have vomiting but are not dehydrated can be managed in the level 4

community with antiemetics, support, reassurance, oral hydration and dietary advice.

If women are unable to tolerate oral antiemetics or oral fluids then ambulatory daycare
management, which provides parenteral fluids, parenteral vitamins (multi and B-complex)30 and
antiemetics, is appropriate if local resources allow. Various regimens have been shown to be
effective.31 A randomised controlled trial (RCT)32 of 98 women showed that ambulatory daycare
management involving intravenous fluids and stepwise increments in antiemetic therapy versus
inpatient management was acceptable to women and resulted in reduced inpatient stay. In a
study of 428 women31 who had ambulatory daycare subcutaneous metoclopramide therapy
(SMT), improvement in symptoms occurred in 89.3%. Those women who failed the SMT regimen
Evidence
(10.7%) had higher mean PUQE scores at the start of ambulatory daycare treatment than those level 2+
for which it was successful (10 3 versus 7.6 2.8 respectively, P < 0.001). Moreover, they were
more likely to have a PUQE score of 13 or higher, they had an earlier gestational age at the start
of SMT (9.7 2.9 weeks versus 11.4 3.2 weeks, P = 0.005) and they were more likely to need
intravenous hydration (91.3% versus 65.2%, P < 0.001). In addition to the SMT regimen, women
received adjuvant therapies at home such as intravenous hydration, subcutaneous ondansetron,
histamine H2 receptor antagonists, and 2.1% received total parenteral nutrition. Ambulatory
daycare management has been successfully and safely set up in units and is associated with high
patient satisfaction.33

Women who have recurrent NVP/HG despite adequate ambulatory daycare treatment should be managed
as inpatients due to the associated complications, in particular electrolyte imbalance and nutritional
deficiencies.

6.2 What therapeutic options are available for NVP and HG?

6.2.1 What is the safety and efficacy of pharmacological agents?

Antiemetics

There are safety and efficacy data for first-line antiemetics such as antihistamines (H1 receptor
antagonists) and phenothiazines and they should be prescribed when required for NVP and HG
C
(Appendix III).

P
Combinations of different drugs should be used in women who do not respond to a single antiemetic.

P
For women with persistent or severe HG, the parenteral or rectal route may be necessary and more
effective than an oral regimen.

Women should be asked about previous adverse reactions to antiemetic therapies. Drug-induced
extrapyramidal symptoms and oculogyric crises can occur with the use of phenothiazines and
B
metoclopramide. If this occurs, there should be prompt cessation of the medications.

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Clinicians should use antiemetics with which they are familiar and should use drugs from different
classes if the first drug is not effective.
B

Metoclopramide is safe and effective, but because of the risk of extrapyramidal effects it should be
B
used as second-line therapy.

There is evidence that ondansetron is safe and effective, but because data are limited it should be
C
used as second-line therapy.

A Cochrane review5 and other systematic reviews and meta-analyses3436 and birth registry data36
have reported on the safety and efficacy of many antiemetics for use in NVP and HG, with no
increased risk of teratogenesis or other adverse pregnancy outcomes. These drugs include: Evidence
antihistamines (histamine H1 receptor antagonists) such as promethazine, cyclizine, cinnarizine, level 2++

doxylamine37 and dimenhydrinate; phenothiazines including prochlorperazine, chlorpromazine

and perphenazine; and dopamine antagonists including metoclopramide38 and domperidone.

Because different drug classes may have different mechanisms of action and therefore synergistic effects,
combinations of drugs from different classes should be used in women who do not respond to a single
antiemetic. Furthermore, persistent vomiting may mean that oral doses of antiemetics are not absorbed and
therefore the intravenous, rectal, subcutaneous or intramuscular routes may be necessary and more
effective.

Due to the risk of extrapyramidal effects with metoclopramide it should be used as second-line
therapy. A review of metoclopramide,39 conducted by the European Medicines Agencys
Committee for Medicinal Products for Human Use, has confirmed the risks of short-term
extrapyramidal disorders and tardive dyskinesia, particularly in young people. The review
recommends metoclopramide should only be prescribed for short-term use (maximum dose of
30 mg in 24 hours or 0.5 mg/kg body weight in 24 hours [whichever is lowest] and maximum
duration of 5 days) and that intravenous doses should be administered by slow bolus injection
over at least 3 minutes to help minimise these risks. Dystonic reactions have been shown to be
significantly less common in nonpregnant patients receiving a slow infusion as opposed to a
bolus injection of 10 mg of metoclopramide.40
Evidence
level 2++
Studies on the safety of ondansetron are mixed. A large retrospective analysis41 of data from the
Danish birth registry of 608 385 pregnancies found no increased risk of major birth defect,
stillbirth, preterm labour or small-for-gestational age. However, a casecontrol study42 with
4524 cases and 5859 controls found a two-fold increased risk of cleft palate (adjusted OR 2.37,
95% CI 1.184.76), although the authors suggest that this association may be due to chance due
to the large number of variables investigated. Data from the Swedish Medical and Birth Register43
demonstrated a small increased risk of cardiovascular defects and cardiac septal defects
(OR 1.62, 95% CI 1.042.14, and risk ratio 2.05, 95% CI 1.193.28, respectively). For these
reasons, the use of ondansetron should be limited to patients who are not adequately managed
on the aforementioned antiemetics and preferably used after the first trimester of pregnancy.

Three small randomised studies4446 have shown ondansetron to be superior to doxylamine and
Evidence
pyridoxine in reducing nausea and vomiting,44 equally effective but with fewer adverse effects level 2+
than metoclopramide45 and more effective at reducing severe vomiting than metoclopramide.46

Suggested antiemetics for UK use are given in Appendix III.

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Pyridoxine

Pyridoxine is not recommended for NVP and HG.

C
There is no association between the degree of NVP at 12 weeks and vitamin B6 levels measured
at 15 weeks.47 A Cochrane review5 concluded that there is a lack of consistent evidence that
pyridoxine is an effective therapy for NVP. Furthermore, a placebo-controlled trial48 of its use in
HG did not demonstrate any improvement in nausea, vomiting or rehospitalisation in 46 women
Evidence
given 20 mg orally three times a day in addition to intravenous fluids, intravenous level 2++
metoclopramide three times a day and oral thiamine compared to the control group given
placebo in addition to standard therapy. A matched nonrandomised study49 demonstrated that
the combination of doxylamine and pyridoxine was significantly more effective than pyridoxine
alone.

Corticosteroids

Corticosteroids should be reserved for cases where standard therapies have failed.
A
Corticosteroids have resulted in dramatic and rapid improvement in case series of women with
refractory HG.50 The results of randomised studies are conflicting51 and the largest study failed
to show improvement in the primary outcome of rehospitalisation (however, both groups also
received metoclopramide and promethazine).52,53 Case selection and route and dose of Evidence
corticosteroid administration may explain the different results, with beneficial results being level 1+

described in more severe cases of HG. A prospective double-blind study54 of 40 women admitted
to intensive care with severe HG demonstrated that daily intravenous hydrocortisone 300 mg was
superior to intravenous metoclopramide in reducing vomiting and recurrence.

Corticosteroids should not be used until conventional treatment with intravenous fluid
replacement and regular antiemetics has failed. The suggested dose is intravenous
hydrocortisone 100 mg twice daily, and once clinical improvement occurs convert to oral
Evidence
prednisolone 4050 mg daily, with the dose gradually tapered until the lowest maintenance dose level 4
that controls the symptoms is reached. In most cases prednisolone needs to be continued until
the gestational age at which HG would have typically resolved and in some extreme cases this
occurs at delivery.29

Diazepam

Diazepam is not recommended for the management of NVP or HG.

B
A randomised trial55 investigated 50 women with HG; they were treated with infusions of saline,
glucose, vitamins and randomly allocated diazepam. While the addition of diazepam to the Evidence
treatment regimen reduced nausea, there was no difference in vomiting between those treated level 1

with or without diazepam.

6.2.2 What is the best rehydration regimen for ambulatory daycare and inpatient management?

Normal saline with additional potassium chloride in each bag, with administration guided by daily
D
monitoring of electrolytes, is the most appropriate intravenous hydration.

Dextrose infusions are not appropriate unless the serum sodium levels are normal and thiamine
D
has been administered.

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The most important intervention is likely to be appropriate intravenous fluid and electrolyte
replacement. There is no evidence to determine which fluid regimen is most appropriate but
given that most women admitted to hospital with HG are hyponatraemic, hypochloraemic,
hypokalaemic and ketotic, it seems appropriate to use normal saline and potassium chloride. Evidence
General adult fluid management guidance can be found in NICE clinical guideline 174.56 level 3

Dextrose-containing solutions can precipitate Wernickes encephalopathy in thiamine-deficient

states (see section 7.1); hence, each day intravenous dextrose is administered, high (e.g. 100 mg)
doses of parenteral thiamine should be given to prevent Wernickes encephalopathy.

Appendix IV provides a summary treatment algorithm for NVP and HG.

6.2.3 Which complementary therapies could be helpful?

Ginger

Ginger may be used by women wishing to avoid antiemetic therapies in mild to moderate NVP.
A
Three systematic reviews5759 have addressed the effectiveness of ginger for NVP. One found four
RCTs that met the criteria and all found that oral ginger was more effective than placebo in
reducing nausea and vomiting.57 The second included a total of ten RCTs, comparing ginger with
placebo (five studies), with vitamin B6 (four studies), and one with dimenhydrinate. Ginger was
superior to placebo and equal to vitamin B6 and dimenhydrinate at improving nausea and Evidence
vomiting.58 The third analysed six studies and 508 subjects randomised to ginger or placebo and level 1++

concluded that ginger was effective.59 Ginger was superior to placebo but less effective than
metoclopramide in a randomised trial including 102 patients with NVP.60 Another group
investigated the effect of ginger biscuits and found them to be better than placebo at reducing
nausea.61 No studies have addressed the effect of ginger in HG under the current definition.

No increased risk of major malformations has been reported with use of ginger;62,63 however, one
Evidence
review64 highlighted potential maternal adverse effects, including an anticoagulant effect, level 2+
stomach irritation and a potential interaction with beta blockers and benzodiazepines.

Acustimulations acupressure and acupuncture

Women may be reassured that acustimulations are safe in pregnancy. Acupressure may improve
NVP.
B

Acupuncture is safe in pregnancy.65 A systematic review66 has addressed the efficacy in NVP of
acustimulations (i.e. acupuncture, acupressure and electrical stimulation) at the pericardium 6
(PC6; Nei Guan) point. PC6 is located about 2.5 finger breadths up from the wrist crease on the
inside of the forearm, between the tendons of palmaris longus and flexor carpi radialis. The
review included 14 studies, and meta-analysis demonstrated acupressure applied by finger
Evidence
pressure or wristband and electrical stimulation both reduced NVP, but acupuncture level 1+
methods did not. There was a placebo effect observed for improvement in nausea (three trials)
and vomiting (five trials) when compared with controls. There is less evidence for a beneficial
effect on vomiting.67 A later systematic review68 found six RCTs including 399 patients
examining the effect of acupressure. Five studies reported positive results and, of these, two
(102 patients) were in women with HG.

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Hypnosis

Hypnotic therapies should not be recommended to manage NVP and HG.

D
A review69 of six studies reporting hypnosis for HG, mainly small case series, concluded that the
Evidence
evidence was not sufficient to establish whether hypnosis (trance induction) is an effective
level 3
treatment.

7. Monitoring and adverse effects

7.1 What complications or adverse effects can occur from NVP and HG and what are their
preventive/management strategies?

P
Urea and serum electrolyte levels should be checked daily in women requiring intravenous fluids.

Histamine H2 receptor antagonists or proton pump inhibitors may be used for women developing
gastro-oesophageal reflux disease, oesophagitis or gastritis.
D

Thiamine supplementation (either oral or intravenous) should be given to all women admitted with
prolonged vomiting, especially before administration of dextrose or parenteral nutrition.
D

Women admitted with HG should be offered thromboprophylaxis with low-molecular-weight heparin

unless there are specific contraindications such as active bleeding. Thromboprophylaxis can be
C
discontinued upon discharge.

Women with previous or current NVP or HG should consider avoiding iron-containing preparations
if these exacerbate the symptoms.
D

In women requiring intravenous fluids, daily monitoring of fluid and serum electrolyte levels is Evidence
important to prevent and treat hyponatraemia and hypokalaemia.29,70 level 4

Recurrent intractable vomiting may lead to gastro-oesophageal reflux disease, oesophagitis or

gastritis. Oesophageal gastroduodenoscopy is safe in pregnancy71 and indicated if there is Evidence
haematemesis or severe epigastric pain. A therapeutic trial with a proton pump inhibitor is level 1+

appropriate for treatment and prevention and is safe in pregnancy.72

A systematic review73 concluded that safety data for histamine H2 receptor antagonists were Evidence
generally reassuring but further studies are needed. level 2+

Wernickes encephalopathy due to vitamin B1 (thiamine) deficiency classically presents with

blurred vision, unsteadiness and confusion/memory problems/drowsiness and on examination
there is usually nystagmus, ophthalmoplegia, hyporeflexia or areflexia, gait and/or fingernose
ataxia. In HG, the presentation tends to be episodic and of slow onset. Wernickes
encephalopathy is a potentially fatal but reversible medical emergency. In the context of HG, it
Evidence
is totally preventable and studies74,75 have stressed the association between Wernickes level 3
encephalopathy and administration of intravenous dextrose and parenteral nutrition. One of
these studies74 reported that complete remission occurred in only 29% and permanent residual
impairment was common. The overall pregnancy loss rate including intrauterine deaths and
terminations was 48%.74 Therefore thiamine supplementation is recommended for all women
with protracted vomiting.

RCOG Green-top Guideline No. 69 13 of 27 Royal College of Obstetricians and Gynaecologists

A retrospective study76 found that the odds ratio for venous thromboembolism with HG was 2.5
(95% CI 23.2). A Canadian study77 using hospital discharge data found an adjusted odds ratio
Evidence
for deep vein thrombosis of 4.4 (95% CI 2.48.4) in women with HG. However, since women level 2+
with HG are only at markedly increased risk while persistently vomiting, thromboprophylaxis can
be discontinued at discharge or when the HG resolves.78

Oral iron can cause nausea and vomiting. In a Canadian prospective cohort study,79 two-thirds
Evidence
of 97 women who discontinued iron supplements reported improvement in their severity of level 2
NVP.

8. Further management

8.1 What is the role of the multidisciplinary team?

In women with severe NVP or HG, input may be required from other professionals, such as midwives,
nurses, dieticians, pharmacists, endocrinologists, nutritionists and gastroenterologists, and a
D
mental health team, including a psychiatrist.

There are many facets to severe NVP and HG and a holistic approach to assessment and treatment should
be adopted.

Dietetic advice can be very helpful to treat or avoid potentially serious complications. Women
requiring enteral or parenteral feeding require input from a gastroenterologist and a Evidence
nutritionist.80 Advice from other specialists such as a pharmacist and endocrinologist may often level 4

be required.

Involvement of a mental health team in the womans care may improve quality of life and the
ability to cope with pregnancy.81 Emotional support and psychological or psychiatric care may Evidence
be required27 with targeted interventions specifically designed to treat mental health issues in level 2

HG, which are a result of HG rather than a cause.8285

8.2 When should enteral and parenteral nutrition be considered and what are the risks to the
mother and fetus?
When all other medical therapies have failed, enteral or parenteral treatment should be considered
D
with a multidisciplinary approach.

There are no defined criteria for parenteral or enteral feeding. Their effectiveness is not well
established. Anecdotally, they can be successful and are often employed as a last resort when all
Evidence
other medical therapy has failed and the only other practical option is termination of the level 2
pregnancy.86,87 Close monitoring of metabolic and electrolyte balance, related complications and
nutritional requirements are needed so a multidisciplinary approach can be employed.

Enteral feeding options to consider include nasogastric, nasoduodenal or nasojejunal tubes, or

percutaneous endoscopic gastrostomy or jejunostomy feeding. Parenteral feeding with a Evidence
peripherally inserted central catheter (PICC line) is often better tolerated than enteral feeding; level 2+

however, it carries a higher risk of infection and vascular perforation.80

There may be resistance to enteral feeding from the patient for cosmetic and psychological Evidence
reasons or for fear of discomfort; however, it is more effective and safer than parenteral feeding.88 level 3

RCOG Green-top Guideline No. 69 14 of 27 Royal College of Obstetricians and Gynaecologists

In some women, intragastric feeding by nasogastric or percutaneous endoscopic gastrostomy
tube increases the risk of nausea and vomiting. It may be tolerated in the short term but not in
protracted HG.89
Evidence
In nasojejunal feeding, the tube is inserted endoscopically to the jejunum and feeding can be level 3

administered by a continuous infusion. One study89 showed that although the majority of women
improved greatly within 48 hours, ongoing vomiting and retching can dislodge gastric and
postpyloric feeding tubes.

Feeding via a percutaneous endoscopic gastrojejunostomy, placed under general anaesthetic in

the second trimester,90 has been shown to be an effective, safe and well-tolerated treatment of
HG. In the majority of women, the tube is removed after delivery. The risk of early dislodgement
is minimised compared with nasoenteric placement.90 Potential complications of percutaneous
endoscopic jejunostomy include tube dislodgement, obstruction or migration, cutaneous or
intra-abdominal abscesses, fistula formation, pneumatosis, occlusion and intestinal ischaemia.
Evidence
Total parenteral nutrition is a complex high-risk intervention; however, it may be useful in level 2+

refractory cases to ensure sufficient calorie intake. It should only be used as a last resort when
all other treatments have failed as it is inconvenient, expensive and can be associated with serious
complications such as thrombosis, metabolic disturbances and infection.27,91 A single
nonrandomised study92 has shown that total parenteral nutrition was associated with a decreased
risk of perinatal morbidity. A strict protocol with careful monitoring is essential when
undertaking total parenteral nutrition.93

8.3 When should termination of pregnancy be considered?

All therapeutic measures should have been tried before offering termination of a wanted pregnancy.
D
The Hyperemesis Education and Research (HER) Foundation in the USA reports that 10% of
pregnancies complicated by HG end in termination in women who would not otherwise have
Evidence
chosen this.94 Pregnancy Sickness Support in the UK found that many of these women have not level 4
been offered the full range of treatments available and fewer than 10% had been offered
steroids.95

Treatment options of antiemetics, corticosteroids, enteral and parenteral feeding, and correction
of electrolyte or metabolic disturbances should be considered before deciding that the only
option is termination of the pregnancy.96,97 A psychiatric opinion should also be sought, and the Evidence
decision for termination needs to be multidisciplinary, with documentation of therapeutic failure level 2

if this is the reason for the termination. Women should be offered counselling before and after
a decision of pregnancy termination is made.

In a survey97 of 808 women who terminated their pregnancies secondary to HG, 123 (15.2%) had
at least one termination due to HG, and 49 (6.1%) had multiple terminations. Prominent reasons
given for the terminations were inability to care for the family and self (66.7%), fear that they or
their baby could die (51.2%), or that the baby would be abnormal (22%). In the same survey, Evidence
women who terminated a pregnancy were more likely to report a negative attitude from their level 4

caregiver. Initiation of a prompt and responsive treatment plan may reduce this.86 Occasionally,
HG or its treatment may lead to life-threatening illness and termination of the pregnancy is seen
as the only option.

RCOG Green-top Guideline No. 69 15 of 27 Royal College of Obstetricians and Gynaecologists

9. Discharge and follow-up

9.1 What discharge and follow-up arrangements should be implemented?

P
Women with NVP and HG should have an individualised management plan in place when they are
discharged from hospital.

Women with severe NVP or HG who have continued symptoms into the late second or the third
trimester should be offered serial scans to monitor fetal growth.
C

At the time of discharge, it is essential that women are advised to continue with their antiemetics
where appropriate and that they know how to access further care if their symptoms and/or signs
recur (e.g. persistent vomiting, dehydration or ketonuria). Earlier treatment may reduce the Evidence
need for hospital admission. Rehydration and a review of antiemetic treatment should ideally be level 2

undertaken in an ambulatory daycare setting.98 Better communication and advice about the
safety of antiemetics may enable general practitioners to adequately support women with HG.95,98

For some women, checking for ketonuria may identify a problem before vomiting is severe,
Evidence
allowing earlier access for rehydration,33 but level of ketones should not be relied upon over level 2+
and above clinical symptoms.99

Advice about patient support groups (e.g. Pregnancy Sickness Support) should be provided as many women
and their partners find this form of support helpful.100102

A follow-up appointment for antenatal care is important in women suffering from HG. Psychological and
social support should be organised depending upon the clinical and social circumstances.

An observational study21 has shown that women with HG and low pregnancy weight gain (less
than 7 kg during pregnancy) are at an increased risk of preterm delivery (adjusted relative risk
3.0, 95% CI 1.94.3) and low birthweight (less than 2500 g; adjusted relative risk 2.8, 95% CI
1.74.3).

Evidence
An Indian study76 demonstrated that excessive vomiting in pregnancy (defined as vomiting that level 2+
lasted beyond 5 months) was significantly (OR 4.48, 95% CI 1.1018.28) associated with
underweight children (in those aged less than 3 years) compared with vomiting lasting less than
5 months. When women with severe HG are considered, it has been shown that those requiring
repeated admissions have an 18% incidence of small-for-gestational-age babies and significantly
lower birthweights than babies of women with HG and single admissions.103

10. What is the effect of NVP and HG in the postnatal period?

10.1 How should we advise about future pregnancies?

Women with previous HG should be advised that there is a risk of recurrence in future pregnancies.
D
Early use of lifestyle/dietary modifications and antiemetics that were found to be useful in the index
pregnancy is advisable to reduce the risk of NVP and HG in the current pregnancy.
C

Reported HG recurrence rates vary, from 15.2% in a Norwegian hospital registry study8 to 81% Evidence
if using self-reported diagnosis.9 level 3

RCOG Green-top Guideline No. 69 16 of 27 Royal College of Obstetricians and Gynaecologists

A Canadian study104 comparing women with NVP (PUQE score of 13 or above) who took
pre-emptive antiemetics before pregnancy or before the onset of symptoms with those who did
not, reported lower recurrence rate of HG in the group that took pre-emptive antiemetics. There
Evidence
was also a significant improvement in the PUQE score of NVP severity compared with the level 2+
previous pregnancy in the pre-emptive group. Women who have experienced severe NVP in a
previous pregnancy may benefit from initiating dietary and lifestyle changes and commencing
antiemetics before or immediately at the start of symptoms in a subsequent pregnancy.104

A small randomised study105 in women with previous NVP demonstrated that pre-emptive treatment with
antiemetics resulted in fewer women with moderate to severe NVP.

11. What is the effect of NVP and HG on quality of life?

A womans quality of life can be adversely affected by NVP and HG and practitioners should address
the severity of a womans symptoms in relation to her quality of life and social situation.
C

Practitioners should assess a womans mental health status during the pregnancy and postnatally
and refer for psychological support if necessary.
D

Women should be referred to sources of psychosocial support.

D
Practitioners should validate the womans physical symptoms and psychological distress.
C
Women should be advised to rest as required to alleviate symptoms.
D
NVP has been reported to reduce quality of life, impairing a womans ability to function on a
day-to-day basis, and negatively affects relationships with her partner and family.81,104,106117
Women with HG are three to six times more likely than women with NVP to have low quality of
life.22 Persistent nausea is the symptom that most adversely affects quality of life.112,118
Furthermore, causes of stress as a consequence of NVP include lack of understanding and
support, inability to eat healthily, grief for loss of normal pregnancy, absence from work, financial
pressures, isolation, inability to care for family, others belief that it is psychosomatic and
reluctance of doctors to treat the condition.24,106,119 Perceived stress positively correlated with
NVP and negatively correlated with social support in a cross-sectional study of 243 women.120 It
has been recommended that social support is necessary as an adjunct to treatment and the circle
of support should be expanded to include family, friends and healthcare professionals.121 A
cohort study106 of 648 women found that having support from at least three other persons was Evidence
protective for NVP. level 2

Clinical assessment should be considered for depression and postnatal depression with
appropriate referral. Depression and poor psychological health were found to be associated with
NVP and HG in numerous studies,82,83,106,107,122129 but resulted from the disease and were not the
cause of HG or NVP. A prospective casecontrol study83 of 32 women compared with 41 matched
controls found that, compared with controls, women with HG had significantly higher levels of
somatisation, depression, anxiety and overall psychological distress even when HG had resolved
to mild NVP.

A cohort study106 of 648 women found that symptoms of major depression are associated with
moderate and severe NVP but prior history of depression is not a determinant.106,130

RCOG Green-top Guideline No. 69 17 of 27 Royal College of Obstetricians and Gynaecologists

Measures that address NVP, poor social support and depression are warranted throughout
pregnancy.106 A prospective cohort study109 of 367 women suggests that practitioners could
improve their management of NVP by addressing symptoms and life situation.

The theory of psychogenic aetiology proposed by Fairweather131 has been severely criticised
for poor methodology and bias.77,132,133 Studies have failed to find a convincing association
Evidence
between a prior history of psychological poor health and risk of suffering from HG,83,124,126,129,134136 level 2+
and poor mental health is a result of the suffering caused by HG rather than being
causal.82,108,122,129,130,136138

Poor psychological health of women with HG is considered as the demoralisation of suffering

from a prolonged, severe chronic illness and in this regard it is similar to mental health problems
suffered in other chronic illnesses.139

The erroneous belief in the psychogenic aetiology of HG is still prevalent among healthcare
professionals101,138142 and poor attitudes towards women contribute to a worse experience for
NVP and HG sufferers.101,121,139,142 A qualitative study of 19 women142 and an online survey of 114
women140,143 found that they struggled to obtain treatment for HG, were dissatisfied with
Evidence
communication during their appointments and found healthcare professionals dismissive and level 4
unsympathetic. A cohort study139 of 808 women demonstrated that women who felt that their
healthcare professional was unsympathetic reported more depression and anxiety. A review
paper137 recommends an integrated approach which addresses both physical and psychological
suffering in HG.

Fatigue is associated with NVP in several studies.112,116,134,140 Rest, particularly napping, is reported
by women to relieve symptoms.115,118,144 A survey143 of 114 women conducted by a volunteer from
Pregnancy Sickness Support found that rest was noted by the majority of respondents with HG Evidence
as being the only effective management strategy aside from antiemetics. Any kind of sensory level 2

stimulation can trigger symptoms, so complete removal from sources of stimulation may be
necessary.143,144

12. Recommendations for future research

Aetiology of NVP and HG.
NVP and HG in relation to pregnancy, birth, and long-term outcomes in mother and baby.
Safety of medication used in NVP and HG.

13. Auditable topics

Women with mild NVP should be managed in the community with antiemetics (100%).
Metoclopramide should not be used as a first-line antiemetic (100%).
Urea and serum electrolyte levels should be checked daily in women with HG requiring intravenous
fluids (100%).
Thiamine supplementation should be given to all women admitted with prolonged vomiting (100%).
Women with HG who are admitted to hospital should receive thromboprophylaxis with
low-molecular-weight heparin, unless there are contraindications (100%).
Women with severe NVP or HG who have symptoms extending into the late second trimester or beyond
should have ultrasound scans to assess fetal growth (100%).

RCOG Green-top Guideline No. 69 18 of 27 Royal College of Obstetricians and Gynaecologists

14. Useful links and support groups
Hyperemesis Education and Research (HER) Foundation [http://www.helpher.org].
Motherisk [http://www.motherisk.org/women/index.jsp].
Pregnancy Sickness Support [http://www.pregnancysicknesssupport.org.uk].
UK Teratology Information Service (UKTIS):
For patients: bumps (best use of medicines in pregnancy). Treating nausea and vomiting in
pregnancy [http://www.medicinesinpregnancy.org/Medicine--pregnancy/NV/].
For professionals: UKTIS. Treatment of nausea and vomiting in pregnancy
[http://www.medicinesinpregnancy.org/bumps/monographs/TREATMENT-OF-NAUSEA-AND-VOMITING-
IN-PREGNANCY/].
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Appendix I: Explanation of guidelines and evidence levels

Clinical guidelines are: systematically developed statements which assist clinicians and patients in
making decisions about appropriate treatment for specific conditions. Each guideline is systematically
developed using a standardised methodology. Exact details of this process can be found in Clinical
Governance Advice No. 1 Development of RCOG Green-top Guidelines (available on the RCOG website
at http://www.rcog.org.uk/green-top-development). These recommendations are not intended to dictate
an exclusive course of management or treatment. They must be evaluated with reference to individual
patient needs, resources and limitations unique to the institution and variations in local populations.
It is hoped that this process of local ownership will help to incorporate these guidelines into routine
practice. Attention is drawn to areas of clinical uncertainty where further research may be indicated.

The evidence used in this guideline was graded using the scheme below and the recommendations
formulated in a similar fashion with a standardised grading scheme.

Classification of evidence levels Grades of recommendations

1++ High-quality meta-analyses, systematic
reviews of randomised controlled trials
or randomised controlled trials with a
very low risk of bias
1+ Well-conducted meta-analyses, systematic
reviews of randomised controlled trials
or randomised controlled trials with a
low risk of bias
1 Meta-analyses, systematic reviews of
randomised controlled trials or
randomised controlled trials with a high
risk of bias
2++ High-quality systematic reviews of case
control or cohort studies or high-quality
casecontrol or cohort studies with a
very low risk of confounding, bias or
chance and a high probability that the
relationship is causal
2+ Well-conducted casecontrol or cohort
studies with a low risk of confounding,
bias or chance and a moderate
probability that the relationship is causal
2 Casecontrol or cohort studies with a
high risk of confounding, bias or chance
and a significant risk that the
relationship is not causal
At least one meta-analysis, systematic review or
A randomised controlled trial rated as 1++, and
directly applicable to the target population; or
A systematic review of randomised controlled
trials or a body of evidence consisting
principally of studies rated as 1+, directly
applicable to the target population and
demonstrating overall consistency of results
A body of evidence including studies rated as
B 2++ directly applicable to the target
population, and demonstrating overall
consistency of results; or
Extrapolated evidence from studies rated as
1++ or 1+
A body of evidence including studies rated as
C 2+ directly applicable to the target population
and demonstrating overall consistency of
results; or
Extrapolated evidence from studies rated as
2++
Evidence level 3 or 4; or
D Extrapolated evidence from studies rated as 2+
Good practice point

P
3 Non-analytical studies, e.g. case reports, Recommended best practice based on the
case series clinical experience of the guideline
4 Expert opinion development group

RCOG Green-top Guideline No. 69 23 of 27 Royal College of Obstetricians and Gynaecologists

Appendix II: Pregnancy-Unique Quantification of Emesis (PUQE) index20

Total score is sum of replies to each of the three questions. PUQE-24 score: Mild 6; Moderate = 712; Severe = 1315.

Motherisk PUQE-24 scoring system

In the last 24 hours, for how long have you Not at all 1 hour or 23 hours 46 hours More than
felt nauseated or sick to your stomach? (1) less (2) (3) (4) 6 hours (5)

In the last 24 hours have you vomited 7 or more 56 times 34 times 12 times I did not
or thrown up? times (5) (4) (3) (2) throw up (1)

In the last 24 hours how many times No time (1) 12 times 34 times 56 times 7 or more
have you had retching or dry heaves (2) (3) (4) times (5)
without bringing anything up?

PUQE-24 score: Mild 6; Moderate = 712; Severe = 1315.

How many hours have you slept out of 24 hours? _______ Why? ____________________________________________________

On a scale of 0 to 10, how would you rate your wellbeing? __________________________________________________________

0 (worst possible) 10 (the best you felt before pregnancy)

Can you tell me what causes you to feel that way? __________________________________________________________________

RCOG Green-top Guideline No. 69 24 of 27 Royal College of Obstetricians and Gynaecologists

Appendix III: Recommended antiemetic therapies and dosages

First line Cyclizine 50 mg PO, IM or IV 8 hourly

Prochlorperazine 510 mg 68 hourly PO; 12.5 mg 8 hourly IM/IV; 25 mg PR daily
Promethazine 12.525 mg 48 hourly PO, IM, IV or PR
Chlorpromazine 1025 mg 46 hourly PO, IV or IM; or 50100 mg 68 hourly PR

Second line Metoclopramide 510 mg 8 hourly PO, IV or IM (maximum 5 days duration)

Domperidone 10 mg 8 hourly PO; 3060 mg 8 hourly PR
Ondansetron 48 mg 68 hourly PO; 8 mg over 15 minutes 12 hourly IV

Third line Corticosteroids: hydrocortisone 100 mg twice daily IV and once clinical improvement occurs,
convert to prednisolone 4050 mg daily PO, with the dose gradually tapered until the lowest
maintenance dose that controls the symptoms is reached

IM intramuscular; IV intravenous; PO by mouth; PR by rectum.

RCOG Green-top Guideline No. 69 25 of 27 Royal College of Obstetricians and Gynaecologists

Appendix IV: Treatment algorithm for NVP and HG

Initial assessment:
Exclude other causes
Record PUQE score
Assess for clinical complications (dehydration, electrolyte imbalance, weight loss)
Offer advice and support

PUQE score 312 and PUQE score of 13 or above Any PUQE score with
no complications: and no complications and complications or
not refractory to unsuccessful ambulatory
Antiemetics in community
antiemetics: daycare management:
Lifestyle and dietary changes
Ambulatory daycare Inpatient management
management until no
ketonuria

Ambulatory daycare Inpatient management:

management:
As for ambulatory daycare
Fast intravenous hydration management plus:
with normal saline and Thromboprophylaxis
potassium (if no Multidisciplinary team
contraindications) approach
Antiemetics (see Appendix III) Consider steroids
Thiamine

RCOG Green-top Guideline No. 69 26 of 27 Royal College of Obstetricians and Gynaecologists

 This guideline was produced on behalf of the Royal College of Obstetricians and Gynaecologists by:
Dr M Shehmar MRCOG, Birmingham; Dr MA MacLean MRCOG, Kilmarnock, Scotland;
Professor C Nelson-Piercy FRCOG, FRCP, London; Dr R Gadsby, University of Warwick, Coventry;
and Dr M OHara, Patient Representative (Pregnancy Sickness Support)
and peer reviewed by:
Dr AM Barnie-Adshead, Nuneaton; Ms E Bennett; British Maternal and Fetal Medicine Society;
Mrs C Dean, Chair of Trustees, Pregnancy Sickness Support; Ms E Dell; Mrs AHD Diyaf MRCOG, Barnstaple;
Mr DI Fraser FRCOG, Norwich; Dr SK Gill, Blainville, Canada; Hyperemesis Education and Research
Foundation; Dr J Jueckstock; Ludwig-Maximilians-University Munich, Germany; Dr CU Kunz, University of
Warwick, Coventry; Dr FPM McCarthy MRCOG, London; Professor I Mylonas, Ludwig-Maximilians-University
Munich, Germany; Dr B OBrien, University of Alberta, Edmonton, Canada; RCOG Womens Network;
Ms C Rivlin; Professor S Robson, Institute of Cellular Medicine, Newcastle University; Royal College of Midwives;
Dr GO Sanu MRCOG, London; Professor H Soltani, Centre for Health and Social Care Research,
Sheffield Hallam University; Ms L Stachow; Dr S Tahmina, Pondicherry Institute of Medical Sciences, India;
Dr LO Walker, School of Nursing, The University of Texas at Austin, USA; Professor H Waterman,
School of Healthcare Sciences, Cardiff University; and Ms E Watford.
Committee lead reviewers were: Dr M Gupta MRCOG, London; and Dr N Potdar MRCOG, Leicester.
The chairs of the Guidelines Committee were: Dr M Gupta1 MRCOG, London; Dr P Owen2 FRCOG, Glasgow,
Scotland; and Dr AJ Thomson1 MRCOG, Paisley, Scotland.
1
co-chairs from June 2014 2until May 2014.

All RCOG guidance developers are asked to declare any conflicts of interest. A statement summarising any
conflicts of interest for this guideline is available from: https://www.rcog.org.uk/en/guidelines-research-services/
guidelines/gtg69/.
The final version is the responsibility of the Guidelines Committee of the RCOG.

The review process will commence in 2019, unless otherwise indicated.

DISCLAIMER

The Royal College of Obstetricians and Gynaecologists produces guidelines as an educational aid to good clinical
practice. They present recognised methods and techniques of clinical practice, based on published evidence, for
consideration by obstetricians and gynaecologists and other relevant health professionals. The ultimate
judgement regarding a particular clinical procedure or treatment plan must be made by the doctor or other
attendant in the light of clinical data presented by the patient and the diagnostic and treatment options available.
This means that RCOG Guidelines are unlike protocols or guidelines issued by employers, as they are not
intended to be prescriptive directions defining a single course of management. Departure from the local
prescriptive protocols or guidelines should be fully documented in the patients case notes at the time the
relevant decision is taken.

RCOG Green-top Guideline No. 69 27 of 27 Royal College of Obstetricians and Gynaecologists